Haemoglobin H disease (– α/– – included) (Q39514)
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Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.02 |
||
| English | Haemoglobin H disease (– α/– – included) |
Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia. |
Statements
CID11:3A50.02
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dki-india-3A50.02
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Concluído
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13 August 2026
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